US9861594B2ActiveUtilityPatentIndex 50
Treatments for attention and cognitive disorders, and for dementia associated with a neurodegenerative disorder
Est. expiryOct 28, 2033(~7.3 yrs left)· nominal 20-yr term from priority
Inventors:KORTAGERE SANDHYA
A61P 25/16A61P 25/14A61P 25/28A61P 25/00A61P 21/02A61K 31/519A61K 45/06A61K 31/4184A61K 31/137A61K 31/4045A61K 2300/00
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References
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Claims
Abstract
The present invention provides a method of treating or preventing an attention and/or cognitive disorder in a subject in need thereof, comprising administering to the subject a compound useful within the invention. The present invention further provides a method of treating or preventing dementia associated with a neurodegenerative disorder in a subject in need thereof, comprising administering to the subject a compound useful within the invention.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A method of treating attention deficit disorder (ADD) or attention deficit hyperactivity disorder (ADHD) in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a compound of formula (I):
wherein:
R 1 , R 2 and R 3 are independently selected from the group consisting of H, cyano, hydroxyl, halo, alkoxy, nitro, C 1-6 alkyl, and carboxy;
R 4 is selected from the group consisting of H and C 1-6 alkyl;
R 5 is selected from the group consisting of H, C 1-6 alkyl, and substituted C 1-6 alkyl; and,
n is 2;
a pharmaceutically acceptable salt or solvate thereof, and any mixtures thereof.
2. The method of claim 1 , wherein administration of the compound improves sustained attention in the subject.
3. The method of claim 1 , wherein in formula (I) R 1 , R 2 and R 3 are independently selected from the group consisting of H, halo, alkoxy, and C 1-6 alkyl.
4. The method of claim 1 , wherein in formula (I) R 5 is selected from the group consisting of H, and C 1-6 alkyl.
5. The method of claim 1 , wherein the at least one compound is selected from the group consisting of: 2-amino-4-(2-chlorophenyl)butan-1-ol; 2-(3-aminohexyl)phenol; 4-(2-chlorophenyl)-2-methylamino-butane; 4-(2-chlorophenyl)-butan-2-amine; 4-(2-fluorophenyl)butan-2-amine; 4-(2-bromophenyl)butan-2-amine; 4-(2-iodophenyl)butan-2-amine; 4-(2-methoxyphenyl)butan-2-amine; 2-(3-aminobutyl)phenol; 3-(3,4-diethoxyphenyl)propan-1-amine; 4-(4-chlorophenyl)butan-2-amine; 4-(4-methoxyphenyl)butan-2-amine; a pharmaceutically acceptable salt or solvate, and mixtures thereof.
6. The method of claim 1 , wherein the composition further comprises at least one drug selected from the group consisting of methylphenidate, dextroamphetamine, dextroamphetamine-amphetamine, lisdexamfetamine, an additional compound that is used to treat ADHD, antidepressant, clonidine, guanfacine, and a salt or solvate thereof.
7. The method of claim 1 , wherein the subject is human.
8. A method of treating dementia associated with a neurodegenerative disease in a subject in need thereof, wherein the neurodegenerative disease comprises at least one selected from the group consisting of Alzheimer's Disease (AD), Huntington's Disease, transmissible spongiform encephalopathies (TSEs), chronic traumatic encephalopathy (CTE) resulting from repeated traumatic brain injuries, and amyotrophic lateral sclerosis (ALS), the method comprising administering to the subject a therapeutically effective amount of a compound of formula (I):
wherein:
R 1 , R 2 and R 3 are independently selected from the group consisting of H, cyano, hydroxyl, halo, alkoxy, nitro, C 1-6 alkyl, and carboxy;
R 4 is selected from the group consisting of H and C 1-6 alkyl;
R 5 is selected from the group consisting of H, C 1-6 alkyl, and substituted C 1-6 alkyl; and,
n is 2;
a pharmaceutically acceptable salt or solvate thereof, and any mixtures thereof.
9. The method of claim 8 , wherein in formula (I) R 1 , R 2 and R 3 are independently selected from the group consisting of H, halo, alkoxy, and C 1-6 alkyl.
10. The method of claim 8 , wherein in formula (I) R 5 is selected from the group consisting of H and C 1-6 alkyl.
11. The method of claim 8 , wherein the at least one compound is selected from the group consisting of: 2-amino-4-(2-chlorophenyl)butan-1-ol; 2-(3-aminohexyl) phenol; 4-(2-chlorophenyl)-2-methylamino-butane; 4-(2-chlorophenyl)-butan-2-amine; 4-(2-fluorophenyl)butan-2-amine; 4-(2-bromophenyl)butan-2-amine; 4-(2-iodophenyl)butan-2-amine; 4-(2-methoxyphenyl)butan-2-amine; 2-(3-aminobutyl) phenol; 3-(3,4-diethoxyphenyl)propan-1-amine; 4-(4-chlorophenyl)butan-2-amine; 4-(4-methoxyphenyl)butan-2-amine; a pharmaceutically acceptable salt thereof, and any mixtures thereof.
12. The method of claim 8 , wherein the composition further comprises at least one drug selected from the group consisting of methylphenidate, dextroamphetamine, dextroamphetamine-amphetamine, lisdexamfetamine, an additional compound that is used to treat ADHD, antidepressants, clonidine, guanfacine, and a salt or solvate thereof.
13. The method of claim 8 , wherein the subject is human.Cited by (0)
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